A recognisable behavioural phenotype associated with terminal deletions of the short arm of chromosome 8

American Journal of Medical Genetics - Neuropsychiatric Genetics

Volumn 74, Issue 5, 1997, Pages 515-520

  Claeys, Ingrid ^a   Holvoet, Maureen ^a   Eyskens, Benedicte ^a   Adriaensens, Peter ^a   Gewillig, Marc ^a   Fryns, Jean Pierre ^a   Devriendt, Koenraad ^a,b  

^a UNIVERSITY HOSPITALS LEUVEN   (Belgium)

^b CENTER FOR HUMAN GENETICS   (Belgium)

Author keywords

Behavioural phenotype; Chromosome 8; Chromosome deletion; Heart malformation

Indexed keywords

ARTICLE; BEHAVIOR DISORDER; CHROMOSOME 8P; CLINICAL ARTICLE; FEMALE; GENE DELETION; HEART VENTRICLE SEPTUM DEFECT; HUMAN; HUMAN CELL; HUMAN TISSUE; KARYOTYPE; MALE; MENTAL DEFICIENCY; MICROCEPHALY; PHENOTYPE; PRIORITY JOURNAL; PULMONARY VALVE STENOSIS;

BEHAVIORAL SYMPTOMS; CHILD; CHILD BEHAVIOR; CHROMOSOME ABERRATIONS; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 8; FEMALE; FOLLOW-UP STUDIES; HEART DEFECTS, CONGENITAL; HUMANS; INFANT; INFANT, NEWBORN; MALE; MENTAL RETARDATION; MICROCEPHALY; PHENOTYPE;

EID: 0030777101     PISSN: 15524841     EISSN: 1552485X     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19970919)74:5<515::AID-AJMG12>3.0.CO;2-F     Document Type: Article

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